Papers - OGI Tomoo
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ALC1/CHD1L, a chromatin-remodeling enzyme, is required for efficient base excision repair
Tsuda Masataka, Cho Kosai, Ooka Masato, Shimizu Naoto, Watanabe Reiko, Yasui Akira, Nakazawa Yuka, Ogi Tomoo, Harada Hiroshi, Agama Keli, Nakamura Jun, Asada Ryuta, Fujiike Haruna, Sakuma Tetsushi, Yamamoto Takashi, Murai Junko, Hiraoka Masahiro, Koike Kaoru, Pommier Yves, Takeda Shunichi, Hirota Kouji
PLOS ONE Vol. 12 ( 11 ) page： e0188320 2017.11
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Transplantation of bioengineered rat lungs recellularized with endothelial and adipose-derived stromal cells
Doi Ryoichiro, Tsuchiya Tomoshi, Mitsutake Norisato, Nishimura Satoshi, Matsuu-Matsuyama Mutsumi, Nakazawa Yuka, Ogi Tomoo, Akita Sadanori, Yukawa Hiroshi, Baba Yoshinobu, Yamasaki Naoya, Matsumoto Keitaro, Miyazaki Takuro, Kamohara Ryotaro, Hatachi Go, Sengyoku Hideyori, Watanabe Hironosuke, Obata Tomohiro, Niklason Laura E., Nagayasu Takeshi
SCIENTIFIC REPORTS Vol. 7 ( 1 ) page： 8447 2017.8
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Phosphorylated HBO1 at UV irradiated sites is essential for nucleotide excision repair
Niida Hiroyuki, Matsunuma Ryoichi, Horiguchi Ryo, Uchida Chiharu, Nakazawa Yuka, Motegi Akira, Nishimoto Koji, Sakai Satoshi, Ohhata Tatsuya, Kitagawa Kyoko, Moriwaki Shinichi, Nishitani Hideo, Ui Ayako, Ogi Tomoo, Kitagawa Masatoshi
NATURE COMMUNICATIONS Vol. 8 page： 16102 2017.7
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An XPA gene splicing mutation resulting in trace protein expression in an elderly patient with xeroderma pigmentosum group A without neurological abnormalities
Takahashi Y., Endo Y., Kusaka-Kikushima A., Nakamaura S., Nakazawa Y., Ogi T., Uryu M., Tsuji G., Furue M., Moriwaki S.
BRITISH JOURNAL OF DERMATOLOGY Vol. 177 ( 1 ) page： 253-257 2017.7
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Calcification in dermal fibroblasts from a patient with GGCX syndrome accompanied by upregulation of osteogenic molecules
Okubo Yumi, Masuyama Ritsuko, Iwanaga Akira, Koike Yuta, Kuwatsuka Yutaka, Ogi Tomoo, Yamamoto Yosuke, Endo Yuichiro, Tamura Hiroshi, Utani Atsushi
PLOS ONE Vol. 12 ( 5 ) page： e0177375 2017.5
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PCNA ubiquitylation ensures timely completion of unperturbed DNA replication in fission yeast
Daigaku Yasukazu, Etheridge Thomas J., Nakazawa Yuka, Nakayama Mayumi, Watson Adam T., Miyabe Izumi, Ogi Tomoo, Osborne Mark A., Carr Antony M.
PLOS GENETICS Vol. 13 ( 5 ) page： e1006789 2017.5
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Analysis of clinical symptoms and ABCC6 mutations in 76 Japanese patients with pseudoxanthoma elasticum. Reviewed
Iwanaga A, Okubo Y, Yozaki M, Koike Y, Kuwatsuka Y, Tomimura S, Yamamoto Y, Tamura H, Ikeda S, Maemura K, Tsuiki E, Kitaoka T, Endo Y, Mishima H, Yoshiura KI, Ogi T, Tanizaki H, Wataya-Kaneda M, Hattori T, Utani A
The Journal of dermatology 2017.2
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A 10-year follow-up of a child with mild case of xeroderma pigmentosum complementation group D diagnosed by whole-genome sequencing. Reviewed
Ono R, Masaki T, Mayca Pozo F, Nakazawa Y, Swagemakers SM, Nakano E, Sakai W, Takeuchi S, Kanda F, Ogi T, van der Spek PJ, Sugasawa K, Nishigori C
Photodermatology, photoimmunology & photomedicine Vol. 32 ( 4 ) page： 174-80 2016.7
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Novel compound heterozygous DNA ligase IV mutations in an adolescent with a slowly-progressing radiosensitive-severe combined immunodeficiency.
Tamura S, Higuchi K, Tamaki M, Inoue C, Awazawa R, Mitsuki N, Nakazawa Y, Mishima H, Takahashi K, Kondo O, Imai K, Morio T, Ohara O, Ogi T, Furukawa F, Inoue M, Yoshiura K, Kanazawa N
Clinical immunology (Orlando, Fla.) Vol. 160 ( 2 ) page： 255-60 2015.10
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XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency.
The Journal of allergy and clinical immunology Vol. 136 ( 4 ) page： 1007-17 2015.10
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SETDB1, HP1 and SUV39 promote repositioning of 53BP1 to extend resection during homologous recombination in G2 cells.
Alagoz M, Katsuki Y, Ogiwara H, Ogi T, Shibata A, Kakarougkas A, Jeggo P
Nucleic acids research Vol. 43 ( 16 ) page： 7931-44 2015.9
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Sensitivity and dose dependency of radiation-induced injury in hematopoietic stem/progenitor cells in mice.
Guo CY, Luo L, Urata Y, Goto S, Huang WJ, Takamura S, Hayashi F, Doi H, Kitajima Y, Ono Y, Ogi T, Li TS
Scientific reports Vol. 5 page： 8055 2015.1
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A rapid, comprehensive system for assaying DNA repair activity and cytotoxic effects of DNA-damaging reagents.
Jia N, Nakazawa Y, Guo C, Shimada M, Sethi M, Takahashi Y, Ueda H, Nagayama Y, Ogi T
Nature protocols Vol. 10 ( 1 ) page： 12-24 2015.1
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Hypomorphic PCNA mutation underlies a human DNA repair disorder.
Baple EL, Chambers H, Cross HE, Fawcett H, Nakazawa Y, Chioza BA, Harlalka GV, Mansour S, Sreekantan-Nair A, Patton MA, Muggenthaler M, Rich P, Wagner K, Coblentz R, Stein CK, Last JI, Taylor AM, Jackson AP, Ogi T, Lehmann AR, Green CM, Crosby AH
The Journal of clinical investigation Vol. 124 ( 7 ) page： 3137-46 2014.7
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PRKDC mutations in a SCID patient with profound neurological abnormalities.
Woodbine L, Neal JA, Sasi NK, Shimada M, Deem K, Coleman H, Dobyns WB, Ogi T, Meek K, Davies EG, Jeggo PA
The Journal of clinical investigation Vol. 123 ( 7 ) page： 2969-80 2013.7
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Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia.
Kashiyama K, Nakazawa Y, Pilz DT, Guo C, Shimada M, Sasaki K, Fawcett H, Wing JF, Lewin SO, Carr L, Li TS, Yoshiura K, Utani A, Hirano A, Yamashita S, Greenblatt D, Nardo T, Stefanini M, McGibbon D, Sarkany R, Fassihi H, Takahashi Y, Nagayama Y, Mitsutake N, Lehmann AR, Ogi T
American journal of human genetics Vol. 92 ( 5 ) page： 807-19 2013.5
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[Molecular cloning and characterisation of UVSSA, the responsible gene for UV-sensitive syndrome].
Ogi T, Nakazawa Y, Sasaki K, Guo C, Yoshiura K, Utani A, Nagayama Y
Seikagaku. The Journal of Japanese Biochemical Society Vol. 85 ( 3 ) page： 133-44 2013.3
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Functional characterization of the novel BRAF complex mutation, BRAF(V600delinsYM) , identified in papillary thyroid carcinoma.
Matsuse M, Mitsutake N, Tanimura S, Ogi T, Nishihara E, Hirokawa M, Fuziwara CS, Saenko VA, Suzuki K, Miyauchi A, Yamashita S
International journal of cancer. Journal international du cancer Vol. 132 ( 3 ) page： 738-43 2013.2
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miR-196a downregulation increases the expression of type I and III collagens in keloid fibroblasts.
Kashiyama K, Mitsutake N, Matsuse M, Ogi T, Saenko VA, Ujifuku K, Utani A, Hirano A, Yamashita S
The Journal of investigative dermatology Vol. 132 ( 6 ) page： 1597-604 2012.6
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Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair.
Nakazawa Y, Sasaki K, Mitsutake N, Matsuse M, Shimada M, Nardo T, Takahashi Y, Ohyama K, Ito K, Mishima H, Nomura M, Kinoshita A, Ono S, Takenaka K, Masuyama R, Kudo T, Slor H, Utani A, Tateishi S, Yamashita S, Stefanini M, Lehmann AR, Yoshiura K, Ogi T
Nature genetics Vol. 44 ( 5 ) page： 586-92 2012.5